Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH5NO3S |
| Molecular Weight | 111.12 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCS(O)(=O)=O
InChI
InChIKey=OBESRABRARNZJB-UHFFFAOYSA-N
InChI=1S/CH5NO3S/c2-1-6(3,4)5/h1-2H2,(H,3,4,5)
| Molecular Formula | CH5NO3S |
| Molecular Weight | 111.12 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Removal of dyes from water using crosslinked aminomethane sulfonic acid based resin. | 2010-08 |
|
| Comparison of zwitterionic N-alkylaminomethanesulfonic acids to related compounds in the Good buffer series. | 2010-04-01 |
|
| The effects of taurine, hypotaurine, and taurine homologs on erythrocyte morphology, membrane fluidity and cytoskeletal spectrin alterations due to diabetes, alcoholism and diabetes-alcoholism in the rat. | 2009 |
|
| The effects of taurine, taurine homologs and hypotaurine on cell and membrane antioxidative system alterations caused by type 2 diabetes in rat erythrocytes. | 2009 |
|
| (Acetato-κO)bis-(2,2'-bipyridyl-κN,N')copper(II)-ethyl sulfate-methyl sulfate (1/0.5/0.5). | 2008-11-20 |
|
| Diaqua-bis(4-bromo-2-formyl-phenolato-κO,O')cobalt(II). | 2008-09-06 |
|
| cis-Aqua-bis(2,4-dichloro-6-formyl-phenolato-κO,O')(N,N-dimethyl-formamide-κO)nickel(II). | 2008-07-26 |
|
| Bis(2,4-dibromo-6-formyl-phenolato-κO,O')copper(II). | 2007-12-06 |
|
| The glycine analogue, aminomethanesulfonic acid, inhibits LPS-induced production of TNF-alpha in isolated rat Kupffer cells and exerts hepatoprotective effects in mice. | 2004-09-17 |
|
| Utilisation of aminomethane sulfonate by Chromohalobacter marismortui VH1. | 2002-01-22 |
|
| Sweetness and enzymatic activity of lysozyme. | 2001-10 |
|
| Inhibition of HIV replication by derivatives of naphthalenedisulfonic acids. | 1990-08 |
|
| Aromatic sulfonic acids as viral inhibitors. Structure-activity study using rhino, adeno 3, herpes simplex, and influenza viruses. | 1971-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:32:46 GMT 2025
by
admin
on
Mon Mar 31 19:32:46 GMT 2025
|
| Record UNII |
OLA224Z482
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
39851
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
209983
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
OLA224Z482
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
DTXSID2065670
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
83791
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
237-649-6
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY | |||
|
13881-91-9
Created by
admin on Mon Mar 31 19:32:46 GMT 2025 , Edited by admin on Mon Mar 31 19:32:46 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
SALT/SOLVATE -> PARENT |
|
